Arrhythmogenic cardiomyopathy and Brugada syndrome: Diseases of the connexome

被引:97
|
作者
Agullo-Pascual, Esperanza [1 ]
Cerrone, Marina [1 ]
Delmar, Mario [1 ]
机构
[1] NYU, Sch Med, Leon H Charney Div Cardiol, New York, NY 10016 USA
来源
FEBS LETTERS | 2014年 / 588卷 / 08期
关键词
Brugada syndrome; Arrhythmogenic right ventricular; cardiomyopathy; Sodium channel; Desmosome; Connexin43; Plakophilin-2; RIGHT-VENTRICULAR CARDIOMYOPATHY; AXON INITIAL SEGMENTS; CHANNEL BETA-SUBUNITS; GAP-JUNCTION PROTEIN; MICROTUBULE PLUS-END; CX43 KNOCKOUT MICE; SODIUM-CHANNEL; ANKYRIN-G; INTERCALATED DISKS; PLAKOPHILIN-2; MUTATIONS;
D O I
10.1016/j.febslet.2014.02.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This review summarizes data in support of the notion that the cardiac intercalated disc is the host of a protein interacting network, called "the connexome'', where molecules classically defined as belonging to one particular structure (e. g., desmosomes, gap junctions, sodium channel complex) actually interact with others, and together, control excitability, electrical coupling and intercellular adhesion in the heart. The concept of the connexome is then translated into the understanding of the mechanisms leading to two inherited arrhythmia diseases: arrhythmogenic cardiomyopathy, and Brugada syndrome. The cross-over points in these two diseases are addressed to then suggest that, though separate identifiable clinical entities, they represent "bookends'' of a spectrum of manifestations that vary depending on the effect that a particular mutation has on the connexome as a whole. (C) 2014 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:1322 / 1330
页数:9
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